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  2. Inborn errors of metabolism - Wikipedia

    en.wikipedia.org/wiki/Inborn_errors_of_metabolism

    Inborn errors of metabolism are often referred to as congenital metabolic diseases or inherited metabolic disorders. [2] Another term used to describe these disorders is "enzymopathies". This term was created following the study of biodynamic enzymology , a science based on the study of the enzymes and their products.

  3. Familial hypocalciuric hypercalcemia - Wikipedia

    en.wikipedia.org/wiki/Familial_hypocalciuric...

    Familial hypocalciuric hypercalcemia (FHH) is an inherited condition that can cause hypercalcemia, a serum calcium level typically above 10.2 mg/dL; although uncommon. [1] It is also known as familial benign hypocalciuric hypercalcemia (FBHH) where there is usually a family history of hypercalcemia which is mild, a urine calcium to creatinine ratio <0.01, and urine calcium <200 mg/day ...

  4. Birth defect - Wikipedia

    en.wikipedia.org/wiki/Birth_defect

    Birth defects are divided into two main types: structural disorders in which problems are seen with the shape of a body part and functional disorders in which problems exist with how a body part works. [3] Functional disorders include metabolic and degenerative disorders. [3] Some birth defects include both structural and functional disorders. [3]

  5. Phenylketonuria - Wikipedia

    en.wikipedia.org/wiki/Phenylketonuria

    An "exchange" system can be used to calculate the amount of Phe in a portion of food from the protein content identified on a nutritional information label. Lower-protein "medical food" substitutes are often used in place of normal bread , pasta , and other grain-based foods, which contain a significant amount of Phe.

  6. Hemolytic disease of the newborn - Wikipedia

    en.wikipedia.org/wiki/Hemolytic_disease_of_the...

    Hemolytic disease of the newborn, also known as hemolytic disease of the fetus and newborn, HDN, HDFN, or erythroblastosis fetalis, [1] [2] is an alloimmune condition that develops in a fetus at or around birth, when the IgG molecules (one of the five main types of antibodies) produced by the mother pass through the placenta.

  7. Mitochondrial DNA depletion syndrome - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_DNA...

    Within weeks of birth they can develop liver failure and the associated jaundice and abdominal swelling, and many neurological problems including developmental delays and regression, and uncontrolled eye movement. Rarely within this class of already rare diseases, symptoms only relating to liver disease emerge later in infancy or in childhood. [5]

  8. AOL Mail

    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. Hyperparathyroidism - Wikipedia

    en.wikipedia.org/wiki/Hyperparathyroidism

    24-hour urinary calcium >250 mg/day in women and >300 mg/day in men (see footnote, below) serum calcium > 1 mg/dl above upper limit of normal; Creatinine clearance > 30% below normal for patient's age; Estimated glomerular filtration rate <60 mL/min/1.73 m2; Bone density > 2.5 standard deviations below peak (i.e., T-score of −2.5) People age < 50